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pro vyhledávání: '"Ta A. Campbell"'
Autor:
Lawrence J. Doey, Jeannine M. Heckmann, S. Rutherfoord, Simon Mead, Jm M. Linehan, J Wadsworth, James M. Beck, S Wroe, Ta A. Campbell, John Collinge, Tef E. F. Webb, Susan Joiner, Andrew T. King
Publikováno v:
Neurology. 69(8)
Background: Humanprion diseases have sporadic, acquired and inherited etiologies and show considerable phenotypic heterogeneity. An individual inherited prion disease offers an opportunity to study the determinants of this clinicopathologic heterogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71a73eff359ac93df8e13ebe89dbc7fd
https://pubmed.ncbi.nlm.nih.gov/17709704
https://pubmed.ncbi.nlm.nih.gov/17709704
